Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98127
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dc.contributor.authorWohland, Thorstenen
dc.contributor.authorKraut, Rachelen
dc.contributor.authorGeifman-Shochat, Susanaen
dc.contributor.authorLauterbach, Timen
dc.contributor.authorManna, Manojen
dc.contributor.authorRuhnow, Mariaen
dc.contributor.authorWisantoso, Yudien
dc.contributor.authorWang, Yaofengen
dc.contributor.authorMatysik, Arturen
dc.contributor.authorOglęcka, Kamilaen
dc.contributor.authorMu, Yuguangen
dc.date.accessioned2013-07-03T02:48:55Zen
dc.date.accessioned2019-12-06T19:50:59Z-
dc.date.available2013-07-03T02:48:55Zen
dc.date.available2019-12-06T19:50:59Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationLauterbach, T., Manna, M., Ruhnow, M., Wisantoso, Y., Wang, Y., Matysik, A., et al. (2012). Weak Glycolipid Binding of a Microdomain-Tracer Peptide Correlates with Aggregation and Slow Diffusion on Cell Membranes. PLoS ONE, 7(12), e51222.en
dc.identifier.issn1932-6203en
dc.identifier.urihttps://hdl.handle.net/10356/98127-
dc.description.abstractOrganized assembly or aggregation of sphingolipid-binding ligands, such as certain toxins and pathogens, has been suggested to increase binding affinity of the ligand to the cell membrane and cause membrane reorganization or distortion. Here we show that the diffusion behavior of the fluorescently tagged sphingolipid-interacting peptide probe SBD (Sphingolipid Binding Domain) is altered by modifications in the construction of the peptide sequence that both result in a reduction in binding to ganglioside-containing supported lipid membranes, and at the same time increase aggregation on the cell plasma membrane, but that do not change relative amounts of secondary structural features. We tested the effects of modifying the overall charge and construction of the SBD probe on its binding and diffusion behavior, by Surface Plasmon Resonance (SPR; Biacore) analysis on lipid surfaces, and by Fluorescence Correlation Spectroscopy (FCS) on live cells, respectively. SBD binds preferentially to membranes containing the highly sialylated gangliosides GT1b and GD1a. However, simple charge interactions of the peptide with the negative ganglioside do not appear to be a critical determinant of binding. Rather, an aggregation-suppressing amino acid composition and linker between the fluorophore and the peptide are required for optimum binding of the SBD to ganglioside-containing supported lipid bilayer surfaces, as well as for interaction with the membrane. Interestingly, the strength of interactions with ganglioside-containing artificial membranes is mirrored in the diffusion behavior by FCS on cell membranes, with stronger binders displaying similar characteristic diffusion profiles. Our findings indicate that for aggregation-prone peptides, aggregation occurs upon contact with the cell membrane, and rather than giving a stronger interaction with the membrane, aggregation is accompanied by weaker binding and complex diffusion profiles indicative of heterogeneous diffusion behavior in the probe population.en
dc.language.isoenen
dc.relation.ispartofseriesPLoS ONEen
dc.rights© 2012 The Authors. This paper was published in PLoS ONE and is made available as an electronic reprint (preprint) with permission of Lauterbach et al. The paper can be found at the following official DOI: [http://dx.doi.org/10.1371/journal.pone.0051222]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.en
dc.subjectDRNTU::Science::Biological sciencesen
dc.titleWeak glycolipid binding of a microdomain-tracer peptide correlates with aggregation and slow diffusion on cell membranesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doi10.1371/journal.pone.0051222en
dc.description.versionPublished versionen
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